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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608940Generated: October 31, 2026

4-Bromothiophenol → S-(4-bromophenyl) 3,3-dimethylthioacrylate

https://huagongshe.com/reaction/1608940

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothiophenolHCID 66049—
Reactant3-Methyl-2-butenoyl chlorideHCID 102394—
SolventTetrahydrofuranHCID 8028—
ProductS-(4-bromophenyl) 3,3-dimethylthioacrylateHCID 15661118—

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice bath cooled solution of 1.92 g (80 mmol) of NaH (obtained from a 60% suspension in mineral oil by 3×15 ml hexane wash) in 30 ml of dry THF was added slowly under argon a solution of 15.1 g (80 mmol) of 4-bromothiophenol in 60 ml of dry THF over 1 hour. The mixture was stirred at 0 degrees C. for a further 30 min and then treated with a solution of 10.1 g (85 mmol) of dimethylacryloyl chloride in 30 ml of dry THF. The cooling bath was then removed and the mixture then stirred at room temperature for 40 h. The reaction mixture was poured into 200 ml of water containing 2 ml of glacial acetic acid and the organic layer was separated. The organic layer was washed with 2×75 ml of water and then dried (MgSO4). The solvent was removed in vacuo to give the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399561
Source datasetuspto-grants-1995_03
ORD IDord-bd3e6980a0394d3e8c4a8a634f97220f
Source noteuspto-grants-1995_03